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HS Code |
136120 |
| Cas Number | 504-02-9 |
| Molecular Formula | C6H8O2 |
| Molecular Weight | 112.13 g/mol |
| Appearance | White to off-white crystalline solid |
| Melting Point | 104-106°C |
| Boiling Point | 227°C at 760 mmHg |
| Density | 1.15 g/cm³ |
| Solubility In Water | Slightly soluble |
| Flash Point | 116°C |
| Refractive Index | 1.509 |
As an accredited 1,3-Cyclohexanedione factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1,3-Cyclohexanedione is supplied in a 100g amber glass bottle with a secure screw cap and chemical safety labeling. |
| Shipping | 1,3-Cyclohexanedione is shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. It should be labeled as a chemical substance and handled according to relevant safety regulations. Ensure containers are upright, secure, and kept away from incompatible materials. Consult the Safety Data Sheet (SDS) for specific shipping requirements. |
| Storage | 1,3-Cyclohexanedione should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from heat sources and direct sunlight. Keep it separate from oxidizing agents and strong bases. Label the container clearly, and avoid moisture contact. Use appropriate personal protective equipment (PPE) when handling and always follow relevant safety guidelines for chemical storage. |
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Purity 99%: 1,3-Cyclohexanedione with purity 99% is used in pharmaceutical synthesis, where it ensures high-yield intermediate production. Melting Point 192°C: 1,3-Cyclohexanedione with melting point 192°C is used in agrochemical formulation, where it provides stable processing conditions. Particle Size <10 microns: 1,3-Cyclohexanedione with particle size less than 10 microns is used in fine chemical manufacturing, where it enhances reactivity in solid-state reactions. Molecular Weight 112.13 g/mol: 1,3-Cyclohexanedione with molecular weight 112.13 g/mol is used in dye intermediate production, where it offers precise formulation control. Stability Temperature 180°C: 1,3-Cyclohexanedione with stability temperature of 180°C is used in polymer modification, where it maintains integrity under heat treatment. Assay ≥98%: 1,3-Cyclohexanedione with assay ≥98% is used in analytical laboratories, where it provides reliable quantification standards. Water Content ≤0.5%: 1,3-Cyclohexanedione with water content ≤0.5% is used in battery electrolyte blends, where it prevents hydrolytic degradation. Low Impurity Profile: 1,3-Cyclohexanedione with a low impurity profile is used in specialty resins synthesis, where it minimizes side-product formation. |
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Every chemist who has spent hours searching for a reliable building block knows the pain of settling for something that just barely fits the bill, especially when it comes to specialty organic compounds. 1,3-Cyclohexanedione isn’t your run-of-the-mill chemical. People often reach for it thanks to its reactivity and versatility, not only because it closes reaction pathways, but because it opens them up. A closer look at its structure — a six-membered cyclohexane ring holding two ketone groups at opposite points — makes its unique behavior in labs clear. Most plain diones or diketones lack the balance of stability and reactivity offered here. Its C6H8O2 formula is simple, but the way the molecule activates position 2 for nucleophilic attack means reactions skip the sluggishness seen with similar cyclic diones.
Most who work with synthesis rely on chemical intermediates that can take a punch and still drive the next step forward. The precise melting point, usually quoted near 104 to 106°C for high-purity grades, is a silent partner to its value; this matters more than some might admit. I remember a chemist friend complaining about the frustration of trialing other diketones, where inconsistent melting and impurities forced repeated re-dosing. In contrast, solid 1,3-Cyclohexanedione generally presents as an off-white powder, easily handled with careful technique and, crucially, available at purities exceeding 98% in reputable supply chains.
In the pharmaceutical world, discovery often takes surprising paths, and researchers need scaffolds that can morph into therapies for rare diseases and common ailments alike. 1,3-Cyclohexanedione acts as a grandmother molecule, helping scientists create everything from anticoagulants to anti-inflammatory drugs. Their choice is no accident. The active methylene group at the 2-position performs reliably in Knoevenagel condensations or Michael additions, both foundational to drug discovery. It won’t always be in the spotlight, but this compound rarely lets the downstream synthesis stall.
Agriculture chemistry stands as another arena where this molecule proves indispensable. Modern herbicides and plant growth regulators need a backbone that holds up to both synthetic steps and field conditions. 1,3-Cyclohexanedione provides a foundation — its robust structure anchors functional groups, lending both durability and reactivity. Many off-patent and emerging crop protection agents quietly build off modifications to this ring system.
For pigment and dye industries, color science only blooms with stable intermediates. Substituted cyclohexanediones form the root of several high-performance pigments. The difference often lies in the purity; even a trace impurity can shade product batches. Labs and processors prize this molecule for its consistency and ease of downstream purification, a detail anybody who’s had a reaction ruined by dirty feedstock can confirm.
Not every diketone offers the same performance. Acetylacetone and dimedone cross the bench in similar roles, but each brings their own baggage. Acetylacetone, for instance, remains highly prone to unwanted tautomerization, especially under heated or basic conditions. Anyone who’s watched their reaction turn to soup knows the cost of losing selective control. Dimedone, bulkier due to its gem-dimethyl groups, narrows the corridor for nucleophilic attack. For synthetic chemists, this means less flexibility and a higher likelihood of disappointing yields.
1,3-Cyclohexanedione finds a middle ground. It isn’t demanding on storage or handling, requiring only dry, cool conditions and avoidance of strong oxidizers. It doesn’t emit the pungent volatility of similar enols. This reliability matters for both academic settings and production-scale plants, where missteps can wipe out an entire batch.
When you line up options side by side, the distinctions grow obvious. Some analogs melt too low, risking sublimation and purity loss. Others resist dissolution in common solvents, especially critical when scaling up to kilos or tons. I’ve seen too many projects delayed because a less suitable analog spent days refusing to dissolve, all while downstream stakeholders waited. Cyclohexanedione, by comparison, stays cooperative with a mild hand — soluble in ethanol or acetone, barely sparking a fuss under routine operations.
Chemists value predictability over glamour. The depth of trust in a compound like 1,3-Cyclohexanedione comes from repeated, unremarkable success. Product quality actually determines whether an experiment will move forward at all. More suppliers now demonstrate their commitment by offering material with certificate of analysis and batch-level traceability. High assay isn’t just a number; it’s a shield against wasted time. Those working under the glare of regulatory oversight increasingly insist on transparent impurity profiles, since downstream drugs or agrochemicals reside under strict scrutiny.
It only takes one bad batch — perhaps loaded with impurities like cyclohexanone or cyclohexanol — to clog a research pipeline. I recall a case from a contract synthesis team, where a simple oversight ended up forcing days of column work. Confidence builds only when a product consistently holds to promised specs, letting teams focus on real innovation rather than troubleshooting someone else’s shortcut.
Safety isn’t just about ticking boxes on a form. We live in an era where mishandling of moderately hazardous solids can cause injury or expose teams to long-term health risk. Compared to many cyclic ketones, 1,3-Cyclohexanedione generally carries manageable hazards. Inhalation or skin contact can irritate, but the lack of strong volatility and absence of severe reactivity allow for careful, straightforward handling. Proper engineering controls, gloves, and a good fume hood do most of the work. Chemistry teachers shaping the next generation find it a pragmatic teaching tool — interesting enough in reactivity to demonstrate essential concepts, not hazardous enough to demand extraordinary precautions.
Sustainability sits high on everyone’s agenda now, from large firms to small contract manufacturers. Making fine chemicals greener takes more than lip service. One upside of cyclohexanedione? Established, scalable syntheses use relatively benign reagents, commonly starting from cyclohexanone, water, and oxidizing agents. Recent process improvements have dialed back the use of heavy metals or noxious solvents, cutting out waste streams that used to raise eyebrows in environmental audits. Some producers now run continuous-flow systems, trimming both resource consumption and emissions while still delivering the same reliable product.
A memorable day in the lab often isn’t marked by grand breakthroughs, but by a series of smooth, manageable steps. Attacking 1,3-Cyclohexanedione with a simple base in a polar solvent feels almost like following a well-tested bread recipe. The methylene bridge activates predictably, letting you build up structures with gentle heating instead of violent reflux. Stirring the solid into solution, I’ve never had that sinking feeling that comes with stubborn, lumpy clumps or disappointing levels of moisture trapped in the powder. In classrooms, students nod their heads when they see crisp melting transitions or sharp NMR signals — signs of a compound behaving as hoped.
After running a couple dozen reactions in my own career, I grew to resent mystery residues. Cyclohexanedione’s clean progress through workup, crystallization, and filtration genuinely makes for less drama and fewer delays. If you’ve spent time in a small synthesis startup, you learn to appreciate how even tiny corners cut on raw material quality can backlog the whole week. This diketone doesn’t force you to lose sleep over stability or annoying shelf-life quirks. It stores well in the warehouse, keeping its promise over months rather than weeks, as long as it’s kept dry.
If good science rests on reproducibility, then dependable reagents deserve more attention. The global market for 1,3-Cyclohexanedione reflects how often new projects come to depend on established intermediates. As drug discovery shifts toward more complex, function-rich “privileged scaffolds,” this molecule’s robust chemistry wins ongoing loyalty. Even as alternatives clamor for space, many synthesis teams return to this diketone because it delivers reliable outcomes when budgets and timelines tighten.
Competition does drive innovation. Suppliers now race to offer ever higher purity grades and more granular impurity profiles, tracing every fingerprint in the supply chain. This clarity supports both agile R&D teams and heavily regulated finish-line projects. The push for digital documentation — with lot traceability embedded in every drum — answers new expectations. It’s no surprise that as customers learn to trust digital records, they demand each batch not only matches tech specs, but aligns with their data-driven quality management systems. This is a crucial shift for industry veterans used to the old handshake system.
Digital tracking also underpins safety improvements. Say a defect emerges or a nonconforming batch appears in trace amounts downstream — robust documentation speeds up root-cause analysis, preventing repeat issues. That’s meaningful progress for plant managers who remember the days of paper logs, chasing missing entries and worrying about inventory mix-ups.
There’s always room to grow, even with trusted molecules. Some supply chains still face last-mile bottlenecks — delays at ports, swings in demand, or hiccups with raw material feedstocks. Companies with global footprints manage these risks by blending local warehousing with continuous communication. Producers who invest in local quality testing and local repackaging centers reduce exposure to surprise quality lapses or transit woes.
Chemical producers feel pressure to track both environmental and social impact. Customers scrutinize more than just specs, they want assurances that material hasn’t cut corners on labor standards or environmental compliance. More suppliers now share audit results and environmental reports, letting end users see how raw material choices tie directly to ESG targets. This trend grows every year. From my side, projects feel smoother knowing that the 1,3-Cyclohexanedione in the bottle represents both a technical solution and a responsible sourcing decision.
Pricing often tracks commodity swings, and forward-looking teams hedge their bets with supply contracts and backup sources rather than chasing the very lowest offer. The lowest-cost kilogram doesn’t always turn into the lowest-cost project, as one misstep in quality or documentation can eat days of troubleshooting budget.
Some compounds thrive as academic curiosities, but those lasting decades in both research and industrial settings must represent more than chemical interest. 1,3-Cyclohexanedione answers the practical needs of synthesis researchers, production chemists, and technology scouts alike. Reactions built on its backbone — whether forging medicines, dyes, or specialty agrochemicals — stand the test of time because of this compound’s consistency, clear-cut purity, and proven flexibility. I’ve met chemists who started working with this molecule in student labs, then returned to it during PhD projects, and continue now in the halls of technical management.
Across universities, startups, and well-established manufacturing plants, trust and predictability earn loyalty far more than flashy campaigns or trendy substitutes. Our industry moves forward on the backs of unassuming workhorses like 1,3-Cyclohexanedione. In this age of digital discovery and heightened scrutiny, its credible track record underscores why the best chemical tools remain both straightforward and quietly sophisticated, firm foundations in every toolkit.
Even as the next wave of synthesis challenges emerge — more demanding regulatory environments, push for green routes, new therapeutic targets — compounds like 1,3-Cyclohexanedione set the standard for reliability. Their legacy isn’t just in ease of handling or predictable reactivity, but in how they underpin trust across decades and generations. For research leaders and plant managers, these details matter. One dependable ingredient streamlines process, empowers innovation, and helps the whole sector keep moving forward.
With transparency, technical support, and sustainability in focus, the best suppliers continue to raise the bar. Nothing replaces the steady assurance that the compound you open today behaves just as it did last year, freeing up skill and creativity for fresh breakthroughs. A workspace stocked with a trustworthy intermediate, one backed by clear specs and clear conscience, is one that keeps science advancing — lab by lab, step by step, batch after batch.